Long Term Efficacy of Antiviral Therapy : Mortality and Incidence of Hepatocellular Carcinoma

Multiple studies have shown that oral antiviral therapies reduced the incidence of hepatocellular carcinoma (HCC) and improved the survival of patients with chronic hepatitis B when compared with that of untreated patients. In particular, entecavir and tenofovir share the qualities of high efficacy in reducing the HBV DNA levels, and they have excellent tolerability and safety. These drugs modified the natural history of liver fibrosis, improve liver function, decrease the incidence of HCC, decrease the need for liver transplantation, and improve survival. Many studies have suggested that long-term antiviral therapy reduces the risk of HCC and liver cirrhosis in patients with chronic hepatitis. The mechanism of these drugs in reducing the risk of HCC is not clear. This article reviews the mechanisms of carcinogenic HBV by conducting a review of the literature on the efficacy of therapy for reducing the risk of HCC. A few recent articles have suggested that tenofovir offers advantages over entecavir in terms of HCC prevention, but these articles have the inherent limitations of observational data. No other head-to-head randomized trials exist. Further randomized studies would help provide stronger evidence of the association between the type of antiviral agent and the HCC outcomes. Only achieving complete viral eradication from the liver will truly decrease the mortality and incidence of HCC.

Medienart:

E-Artikel

Erscheinungsjahr:

2019

Erschienen:

2019

Enthalten in:

Zur Gesamtaufnahme - volume:74

Enthalten in:

The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi - 74(2019), 5 vom: 25. Nov., Seite 251-257

Sprache:

Koreanisch

Beteiligte Personen:

Lee, Hyun Woong [VerfasserIn]

Links:

Volltext

Themen:

5968Y6H45M
5Z93L87A1R
99YXE507IL
Antiviral Agents
Antiviral agents
Carcinoma
Chronic
Entecavir
Guanine
Hepatitis B
Hepatocellular
Journal Article
Mortality
Review
Tenofovir

Anmerkungen:

Date Completed 15.05.2020

Date Revised 15.05.2020

published: Print

Citation Status MEDLINE

doi:

10.4166/kjg.2019.74.5.251

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM303679506